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4-苯基丁酸对内质网应激的抑制对牙周炎具有治疗作用:大鼠实验研究

Inhibition of Endoplasmic Reticulum Stress by 4-Phenyl Butyric Acid Presents Therapeutic Effects on Periodontitis: Experimental Studies and in Rats.

作者信息

Feng Yang, Zhang Rong, Wang Yi-Rong, Chen Fei, Luo Qiang, Cai Chuan, Jiao Yang, Xue Peng

机构信息

Institute of Stomatology, The First Medical Center, Chinese PLA General Hospital, Beijing 100853, China.

Department of Traditional Chinese Medicine and Acupuncture, The Second Medical Centre, Chinese PLA General Hospital, National Clinical Research Center for Geriatric Diseases, Beijing 100853, China.

出版信息

Stem Cells Int. 2021 Mar 3;2021:6618943. doi: 10.1155/2021/6618943. eCollection 2021.

Abstract

This study investigated the probable mechanisms of endoplasmic reticulum (ER) stress involved in periodontitis and . We isolated periodontal ligament stem cells from periodontitis patients and healthy controls (P-PDLSCs and H-PDLSCs). To further simulate the periodontal microenvironment in patients, lipopolysaccharide (LPS) was used to treat H-PDLSCs. The results showed that periodontitis-related inflammation gave rise to the upregulated expression levels of ER stress representative genes including , , , and . In contrast, the treatment of 4-phenyl butyric acid (4-PBA) remarkably suppressed ER stress and supported cell viability. The increased secretion of proinflammatory factors like TNF-, IL-1, and IL-6 and the activation of NF-B pathway were also attenuated by 4-PBA treatment. Moreover, 4-PBA treatment restored the impaired osteogenic differentiation ability of PDLSCs, as demonstrated by the upregulated expression levels of Runx2 and OCN as well as the enhanced Alizarin red staining. Local administration of 4-PBA could rescue alveolar bone resorption of LPS-induced periodontitis rats. Thus, our findings suggested ER stress might act as a promising therapeutic target against periodontitis.

摘要

本研究调查了内质网(ER)应激参与牙周炎的可能机制。我们从牙周炎患者和健康对照者中分离出牙周膜干细胞(P-PDLSCs和H-PDLSCs)。为了进一步模拟患者的牙周微环境,使用脂多糖(LPS)处理H-PDLSCs。结果显示,牙周炎相关炎症导致ER应激代表性基因(包括 、 、 和 )的表达水平上调。相反,4-苯基丁酸(4-PBA)处理显著抑制了ER应激并维持了细胞活力。4-PBA处理还减弱了促炎因子如TNF-、IL-1和IL-6的分泌增加以及NF-κB通路的激活。此外,4-PBA处理恢复了PDLSCs受损的成骨分化能力,Runx2和OCN的表达水平上调以及茜素红染色增强证明了这一点。局部给予4-PBA可以挽救LPS诱导的牙周炎大鼠的牙槽骨吸收。因此,我们的研究结果表明ER应激可能是对抗牙周炎的一个有前景的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c13/7946453/9e6ad91aaef8/SCI2021-6618943.001.jpg

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